Abstract
Rational engineering of enzymes involves introducing key amino acids guided by a knowledge of protein structure to effect a desirable change in function. To date, all successful attempts to change specificity have been limited to substituting individual amino acids within a protein fold. However, the infant field of protein engineering will only reach maturity when changes in function can be generated by rationally engineering secondary structures. Guided by x-ray crystal structures and molecular modeling, site- directed mutagenesis has been used to systematically invert the coenzyme specificity of Thermus thermophilus isopropylmalate dehydrogenase from a 100- fold preference for NAD to a 1000-fold preference for NADP. The engineered mutant, which is twice as active as wild type, contains four amino acid substitutions and an α-helix and loop that replaces the original β-turn. These results demonstrate that rational engineering of secondary structures to produce enzymes with novel properties is feasible.
Original language | English (US) |
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Pages (from-to) | 12171-12176 |
Number of pages | 6 |
Journal | Proceedings of the National Academy of Sciences of the United States of America |
Volume | 93 |
Issue number | 22 |
DOIs | |
State | Published - Oct 29 1996 |
Keywords
- NAD
- NADP
- protein engineering
- specificity